Hydroxyzine hydrochloride NDC 68788-7854

Product information

Brand name (proprietary)

Hydroxyzine hydrochloride

Generic name (nonproprietary)

hydroxyzine hydrochloride

Active ingredients

Hydroxyzine hydrochloride — 25 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Preferred Pharmaceuticals Incl

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 204279

Marketing start

Jan 29, 2021

Listing expires

Dec 31, 2027

Other FDA classes

Histamine Receptor Antagonists (Mechanism)

Identifiers

Product ID 68788-7854_e3a724e1-eb77-4678-898d-d3ad022b19b8SPL ID e3a724e1-eb77-4678-898d-d3ad022b19b8SPL set ID 63fdf791-1a58-45ba-8ef2-15b80bb24f23RxCUI 995258UNII 76755771U3

Pharmacologic class

Antihistamine

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468788785403 followed by a unit qualifier and the quantity Copy

Package 68788-7854-03. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 204279

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

Showing 20 of 39.